Quantalx Neroscience is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Quantalx Neroscience - FDA 510(k) Cleared Devices
Recent clearances: Delphi Amplifier
1
Total
1
Cleared
0
Denied
Quantalx Neroscience has 1 FDA 510(k) cleared medical devices. Based in Kfar Sava, IL.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Quantalx Neroscience Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Quantalx Neroscience
1 devices